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Methylmalonic Acidemia with Novel MUT Gene Mutations

A 5-year-old boy presented with recurrent episodes of fever, feeding problems, lethargy, from the age of 11 months, and poor weight gain. He was admitted and evaluated for metabolic causes and diagnosed as having methylmalonic acidemia (MMA). He was treated with vit B12 and carnitine supplements and...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: Inusha Panigrahi, Savita Bhunwal, Harish Varma, Simranjeet Singh
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: Wiley 2017-01-01
Σειρά:Case Reports in Genetics
Διαθέσιμο Online:http://dx.doi.org/10.1155/2017/8984951
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